BEUDAMED
    224 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    OSTEOPHIL BETA-TCP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bartels

    FDA UDI
    CLARK LABORATORIES, INC.·05391516747271·Tissue Culture Refeeding Medium

    Trab-X SB Synthetic Bone Matrix

    FDA UDI
    CYTOPHIL, INC.·00856509002584·Synthetic bone graft substitute in particulate ...

    KNEE MODULE FOR THE STEALTHSTATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    TST CONTROL INTEGRATOR FOR STEAM STERILIZERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GMK-REVISION FEMUR REVISION PS SIZE 6 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 12, 2017

    GMK-HINGE FIXED TIBIAL TRAY SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·August 28, 2019

    GMK HINGE FEMUR SIZE 5 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2017

    GMK-REVISION FEMUR REVISION PS SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 19, 2019

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·February 25, 2020

    GMK HINGE FEMUR SIZE 2 RIGHT

    FDA Adverse Event
    Injury ·Product code KRO·September 12, 2014

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 29, 2025

    GMK-REVISION FEMUR REVISION PS SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 6, 2018

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 3+ RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 12, 2017

    UNKNOWN BONE CEMENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LOD·May 9, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 19, 2014

    CVC SET: 2-LUMEN 4 FR X 13 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQY·May 4, 2011

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·November 6, 2019

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 30, 2019